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The Effects of a Nutrition Supplement on Health Related Quality of Life

The Effects of a Nutrition Supplement on Health Related Quality of Life

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04499560
Enrollment
160
Registered
2020-08-05
Start date
2020-08-03
Completion date
2020-12-31
Last updated
2021-02-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Symptom, Health, Subjective, Inflammation, Sleep, Stress

Keywords

immune health, prevention, phytonutrients, superfoods, antioxidant, essential oils

Brief summary

The purpose of this study is to evaluate the health related benefits of a superfoods nutrition supplement on health related quality of life.

Detailed description

After being informed about the study, participants will provide informed consent and be randomized to one of two groups: intervention or control. Those in the intervention group will consume two ounces of a superfoods drink each morning for 60 days. Outcomes will be assessed at baseline, on day 30 and on day 60.

Interventions

DIETARY_SUPPLEMENTSupplement Drink

Superfoods based nutritional supplement

Sponsors

Young Living Essential Oils
CollaboratorUNKNOWN
Nutraceuticals Research Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* otherwise healthy * adults living in the US * is practicing adequate contraception or is abstaining from all activities which could result in pregnancy * understands and agrees to comply with study procedures * provides informed consent

Exclusion criteria

* smoker * pregnant or may become pregnant * currently breastfeeding * currently taking antioxidant supplements * underlying chronic health conditions * COVID-19 diagnosis * demonstrated inability to comply with study procedures * history of allergy to citrus or berry fruits * has participated in an interventional clinical study within 31 days prior to enrollment

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in sleep quality on Pittsburgh Sleep Quality Index (PSQI) on Day 60Baseline and day 60The PSQI is a validated, self reporting instrument assessing sleep. Possible scores range from 0 to 21 with higher scores indicating lower quality sleep. The instrument contains 19 items.
Change from baseline in general wellbeing on the Physical Health Questionnaire (PHQ) on Day 60Baseline and day 60The PHQ is a validated, self reporting instrument assessing general wellbeing through sleep, respiratory health, headache, and gastrointestinal symptoms. Possible scores on each item range from 1 to 7 with higher scores indicating greater frequency of symptoms. The instrument contains 14 items.
Change from baseline in cognitive wellness on the Self Report Measure of Cognitive Abilities (SRMCA) on Day 60Baseline and day 60The SRMCA is a validated, self reporting instrument assessing cognitive wellbeing. Possible scores range from 0 to 27 with higher scores indicating greater cognitive wellbeing. The instrument contains 44 items.
Number of days with any cold symptoms as defined by the Jackson Symptom Score on day 60.Day 60The Jackson Symptom Score is a validated, self reporting instrument which contains 8 cold and flu symptoms. Scores range from 0 (no symptoms) to 8 (every one of the listed symptoms.)
Change from baseline in stress on the Perceived Stress Scale (PSS) on Day 60Baseline and Day 60The PSS is a validated, self reporting instrument assessing perceived stress. Possible scores range from 0 to 40 with higher scores indicating higher stress levels. The instrument contains ten items.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026